National Council on Disability


Chapter 3. Qualitative Research: Interviews with Key Informants from the Disability Community



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Chapter 3. Qualitative Research: Interviews with Key Informants from the Disability Community


In this chapter, we report the results of interviews conducted with 16 key informants from ten states between March and April 2015. The interviews were designed to explore the early effects of state-level ACA implementation choices on people with disabilities and to provide preliminary data to aid in the development of research questions, policies, and tracking of the ongoing impacts of the ACA on people with disabilities. At this stage in implementation, five years since the ACA was signed into law, our findings reflect only early impressions of the ACA’s impact on people with disabilities. Given the limited data on this topic, the key-informant interviews offer valuable insights on the experiences of people with disabilities with QHPs, expanded Medicaid for low-income adults, health care coverage enrollment processes, changes to long-term services and supports, and other health systems changes.75

Selection of States and Participants


We selected participants from states with diverse ACA implementation approaches concerning Medicaid expansion, insurance Marketplaces, and state options specific to services for people with disabilities. First, we compiled information on state implementation approaches for all 50 states plus the District of Columbia and grouped them into broad categories (for example, states that expanded Medicaid versus those that have not expanded eligibility). Second, we identified states where research team members had knowledge of or existing connections with disability leaders or organizations. We then used this information to compile a list of 13 states, prioritized on the basis of maximum variation in implementation choices, availability of existing contacts, and distribution across geographic regions of the United States. After obtaining feedback on state selection from National Council on Disability members, we conducted outreach to contacts in each target state.

We interviewed participants from ten states; the ACA implementation characteristics for each participating state are summarized in Table 2. Half of the states (N=5) opted to expand Medicaid to cover low-income adults up to 138 percent of the FPL. Two of the states pursued a nontraditional Medicaid expansion plan using Section 1115 waivers (for example, Medicaid funds used as premium assistance for newly eligible adults to purchase QHPs), and three of the states had not expanded Medicaid. We classified states’ success with Marketplace enrollment using table 1 in Blumberg et al., which defines “high,” “medium,” and “low” success rates, respectively, on the basis of enrollment of more than 25 percent, from 15 percent to 25 percent, and under 15 percent of the state’s target population (defined as pre-reform non-group insurance enrollees and uninsured individuals who are ineligible for public insurance or affordable employer-based coverage).76



Table 2. State ACA Implementation Characteristics of States Included in the Interviews at the Time of Interviewee Selection (January 2015)

State

Medicaid Expansion

Enrollment Success*

States Options Relevant to People with Disabilities**

Exchange Type

Arkansas

Yes, nontraditional

Medium

CFC***

State Partnership

California

Yes

High

CFC & DD

State-Based

Colorado

Yes

High

DD

State-Based

Florida

No

High

None

Federally Facilitated

Kansas

No

Medium

None

Federally Facilitated

Montana

No

Medium

CFC

Federally Facilitated

North Dakota

Yes

Low

None

Federally Facilitated

Oregon

Yes

Medium

CFC & DD***

Federally Supported State-Based

Pennsylvania

Yes, nontraditional****

Medium

None

Federally Facilitated

New York

Yes

High

DD

State-Based

Notes:

* Enrollment success is based on Blumberg et al., table 1.77 The original table shows each state’s current enrollment (as of April 2014) in the Marketplace as a percentage of the target population (defined as pre-reform non-group insurance enrollees and uninsured individuals who are ineligible for public insurance or affordable employer-based coverage). We have classified states into three broad categories of enrollment success using this percentage: low (below 15 percent), medium (15 percent to 25 percent), and high (above 25 percent).

** Community First Choice (CFC): States participating in the Section 1915(k) Community First Choice State Plan Option.78 Dual Demonstrations (DD): State participating in the State Demonstrations to Integrate Care for Dual Eligible Individuals.79

*** Participants provided different information on implementation status.

****The state’s original proposal for Medicaid expansion involved a Section 1115 waiver. However, the state’s new governor now plans to implement a standard Medicaid expansion.

Most states had medium or high Marketplace enrollment success (N=5 and N=4, respectively); one state had low enrollment success. For LTSS options specific to services for people with disabilities, the CFC option was being implemented by four of the states shown in the table, and the State Demonstrations to Integrate Care for Dual Eligible Individuals, or “Duals Demonstration,” option was being implemented in four of the states shown in the table. The states also represented four Marketplace types: federally facilitated (N=5), state-based (N=3), state partnership (N=1), and federally supported, state-based Marketplaces (N=1).

Within each identified state, we purposely selected participants to provide broad perspectives on experiences with the ACA among people with disabilities. We targeted state-based community leaders (not employees of state agencies) who worked or volunteered for disability organizations and were familiar with ACA implementation in their state. In selecting our participant sample, we aimed to identify participants who have disabilities themselves and displayed diversity across functional categories of disability and demographic characteristics. We created an initial list of potential participants and organizational affiliations, then obtained feedback and additions from study partners and the National Council on Disability. In states where we did not have an individual identified who met the participant selection criteria, we identified and contacted individuals and organizations with knowledge of key disability stakeholders in the state to ask for recommendations for potential interviewees. Potential participants were then contacted by the project team by e-mail and phone and invited to participate. In total, we contacted more than 60 individuals in the outreach process. Among state-based disability rights leaders who declined to participate and were themselves people with disabilities, limited knowledge of the ACA was a commonly cited reason.

Overall, we were able to identify 16 suitable interview participants for the ten state-based interviews. Four interviews had one interviewee each and the other six had two interviewees each. Table 3 displays characteristics of the 16 interview participants. Half (N=8) of them had personal disability experience, either directly (N=5) or through an immediate family member (N=2) or other individual (N=1) for whom the participant was caring. Participants’ personal disability experience included physical (N=5), vision (N=1), hearing (N=1), developmental (N=1), and other (N=1) disabilities; two participants indicated two disability categories, and one participant with personal disability experience did not disclose a disability category. In most of the interviews—in eight out of ten states—at least half of the interviewees had a personal disability experience.



All 16 participants had rich professional experience working on behalf of people with disabilities. Participants were engaged in both direct services and advocacy as well as policy and systems changes to improve health care access for this population. Most participants worked or volunteered for a cross-disability organization (that is, organizations working for the benefit of all people with disabilities), and one participant worked for a disability organization that served individuals with physical, cognitive/intellectual, and mental health/psychiatric disabilities. Participants worked for or were affiliated with many organizational types, including disability rights organizations, centers for independent living, legal aid, and disability and health programs. Most of these organizations (N=10) were accountable to people with disabilities through boards, advisory councils, and memberships in which people with disabilities and their caretakers constituted a majority. The majority of participants were involved in policy advocacy to improve health care for people with disabilities, both prior to the ACA and in recent years focusing on ACA implementation issues. Several participants had served on committees or provided input on state policy related to Medicaid reform and ACA implementation.

Table 3: Participant Characteristics

Characteristic

Number (Percent)

Gender




Male

7 (44 percent)

Female

9 (56 percent)

Age




Mean (Range)

53 years (32 years to 72 years)

Race/ethnicity




Non-Hispanic White

12 (75 percent)

Non-Hispanic Black

1 (6 percent)

Asian

1 (6 percent)

No response

2 (13 percent)

Personal disability experience*




Physical

5 (31 percent)

Vision/Hearing

2 (13 percent)

Developmental

1 (6 percent)

Other

1 (6 percent)

Unspecified

1 (6 percent)

None

8 (50 percent)

Organizational affiliation




Cross-disability organization

15 (94 percent)

Other disability organization

1 (6 percent)

Note: *Personal disability experience includes participants who have disabilities themselves or have an immediate family member or other individual for whom the participant was caring who has a disability.
Five participants provided legal-based services related to access to health care for people with disabilities through their work for legal services organizations and state protection and advocacy organizations. Nearly half of participants (N=7) had a background in providing other direct services, including experience with centers for independent living, special education, habilitative and rehabilitative services, community mental health services, services for families of children with disabilities and special health care needs, peer support, and health coverage advocacy for people with disabilities. Four participants served as health care Navigators, assisting people with disabilities enrolling in coverage under the ACA; two of those who served as Navigators also held leadership roles in their respective Navigator programs.


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